Canonical Allele Identifier: CA229613548

Gene: LINC02744

Linked Data

• dbSNP Id: rs535380636
• gnomAD v2: 11-119863542-G-A
• gnomAD v3: 11-119992833-G-A
• gnomAD v4: 11-119992833-G-A
• MyVariant Identifiers: chr11:g.119863542G>A (hg19) ; chr11:g.119992833G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119992833G>A , CM000673.2:g.119992833G>A	GRCh38
NC_000011.9:g.119863542G>A , CM000673.1:g.119863542G>A	GRCh37
NC_000011.8:g.119368752G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_948086.1:n.553C>T
XR_948087.1:n.199+1761C>T
XR_948088.1:n.40C>T
XR_948089.1:n.40C>T
XR_948090.1:n.176+1761C>T
XR_948091.1:n.177+1761C>T
XR_948092.1:n.40C>T
XR_948093.1:n.177+1761C>T
XR_948094.1:n.175+1761C>T
XR_948095.1:n.40C>T
XR_948096.1:n.174+1761C>T
XR_002957267.1:n.2092C>T
XR_948086.2:n.645C>T
XR_948087.2:n.346+1761C>T
XR_948088.3:n.2095C>T
XR_948089.3:n.2093C>T
XR_948090.2:n.338+1761C>T
XR_948091.2:n.340+1761C>T
XR_948092.3:n.2094C>T